EP0645096B1 - Mannitol pulvérulent de friabilité modérée et son procédé de préparation - Google Patents

Mannitol pulvérulent de friabilité modérée et son procédé de préparation Download PDF

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Publication number
EP0645096B1
EP0645096B1 EP94402134A EP94402134A EP0645096B1 EP 0645096 B1 EP0645096 B1 EP 0645096B1 EP 94402134 A EP94402134 A EP 94402134A EP 94402134 A EP94402134 A EP 94402134A EP 0645096 B1 EP0645096 B1 EP 0645096B1
Authority
EP
European Patent Office
Prior art keywords
mannitol
microns
less
pulverulent
preferentially
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
EP94402134A
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German (de)
English (en)
French (fr)
Other versions
EP0645096A1 (fr
Inventor
Michel Serpelloni
Jean-Philippe Boonaert
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Roquette Freres SA
Original Assignee
Roquette Freres SA
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
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Application filed by Roquette Freres SA filed Critical Roquette Freres SA
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Classifications

    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00—Medicinal preparations characterised by special physical form
    • A61K9/20—Pills, tablets, discs, rods
    • A61K9/2004—Excipients; Inactive ingredients
    • A61K9/2013—Organic compounds, e.g. phospholipids, fats
    • A61K9/2018—Sugars, or sugar alcohols, e.g. lactose, mannitol; Derivatives thereof, e.g. polysorbates
    • A—HUMAN NECESSITIES
    • A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23L—FOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
    • A23L27/00—Spices; Flavouring agents or condiments; Artificial sweetening agents; Table salts; Dietetic salt substitutes; Preparation or treatment thereof
    • A23L27/30—Artificial sweetening agents
    • A23L27/33—Artificial sweetening agents containing sugars or derivatives
    • A23L27/34—Sugar alcohols
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C31/00—Saturated compounds having hydroxy or O-metal groups bound to acyclic carbon atoms
    • C07C31/18—Polyhydroxylic acyclic alcohols
    • C07C31/26—Hexahydroxylic alcohols

Definitions

  • the subject of the present invention is a pulverulent mannitol of moderate friability furthermore having a low density and a particular particle size.
  • sucrose and lactose used in particular as an excipient in the dry forms such as, for example, capsules, dissolving powders, powdery nutritive preparations and tablets. These sugars are also used in crystallized form in the industrial preparation of drinkable solutions and suspensions.
  • sucrose for its part, also uses significant quantities of sucrose for similar reasons, that is to say in the crystallized state in the dry forms which are the sweet foods to be dispersed and diluted such as for example powdered drinks and desserts, either in the solute state as in the preparation of liquid drinks.
  • sucrose finds certain use as a support in various industries such as that of additives intended in particular for the food and pharmaceutical fields.
  • additives can be flavors, colors, intense sweeteners, vitamins, active ingredients or even protein materials such as amino acids, and enzymes.
  • Sorbitol has the advantage of being among these three polyols, the cheapest product. This explains its high frequency of use. This is an excellent excipient, particularly in compression, due to its particular ability to crystallize in the form of crystals in directly compressible needles.
  • Mannitol obtained by crystallization in water also has, due to its very compact crystal structure, poor ability to dissolve. This is the case even when the product is finely ground because then the particles are electrostatically charged and form agglomerates which dissolve only very slowly.
  • This low rate of solubilization although considered as an advantage in certain particular applications, is in the cases in which we are interested here, always considered as a major drawback hindering its use.
  • relatively pure means a richness in mannitol, calculated relative to the amount of sugars or polyols present, of at least 90%.
  • sugars and polyols is meant in the present invention the mono and disaccharides in hydrogenated form or not.
  • the sorbitol marketed by the applicant under the brand NEOSORB R 20/60 DC having a high density, has a friability of 54% in the test described in French patent No. 2,571,045 while a atomized sorbitol like that sold for example by the company Merck under the brand KARION R Instant, with a significantly lower density, for its part, for a particle size close to and under the same measurement conditions, a higher friability, close to 75 %.
  • test I which consists in subjecting the particles to test with a mechanical action in a device called a friabilimeter.
  • a friabilimeter an apparatus of the ERWEKA TAP brand manufactured by the company ERWEKA (6056 HEUSENSTAMM - RFA) is used rotating at a uniform speed of rotation of 25 revolutions / minute, and into which 5 identical steel balls of a diameter have been introduced. 17 mm and a weight of 18.87 g.
  • a quantity of 15 g of product having a particle size between 100 to 200 microns is introduced into the crushing chamber of this friabilimeter, then the apparatus is rotated for 15 minutes.
  • the pulverulent mannitol according to the invention present in this test I, a moderate and not excessive friability, that is to say between approximately 40 and 80%.
  • a moderate and not excessive friability that is to say between approximately 40 and 80%.
  • the mannitol in accordance with the invention has a particularly low apparent density, that is to say between approximately 300 and approximately 525 g / l, preferably 350 to 510 g / l and more preferably between 400 and 495 g / l.
  • the pulverulent mannitol according to the invention has, so as to have the flow and dissolution properties characteristic of an ideal support or excipient, which does not generate dust in workshops, a very specific and centered grain size. It always contains less than around 30% of particles smaller than 75 microns.
  • the preferred pulverulent mannitol contains less than 25% or even less than 15%; the ideal being, although this is more difficult to obtain, a pulverulent mannitol containing not more than 10% and better still not more than 5% of particles smaller than 75 microns.
  • the pulverulent mannitol according to the invention is preferably almost devoid of particles smaller than 40 microns, these being the most polluting and the most explosive.
  • the product according to the invention is virtually free of particles larger than 315 microns so that its ability to dissolve in water is excellent.
  • the pulverulent mannitol according to the invention generally contains very small amounts of water. This content is preferably less than 1% and more preferably still less than 0.3%.
  • the pulverulent mannitol of the present invention can comprise substances other than sugars or polyols in more or less quantity depending on the destination that it is made of.
  • dyes, flavors, perfumes, pharmaceutical or veterinary principles preservatives, acids and their salts, intense sweeteners, vitamins, materials fatty, protein materials such as amino acids, enzymes or gelatins, gums such as arabic and tragacanth gum, basic gums of the chewing gum type, cellulose fibers, cellulose and its derivatives such as, for example, hydropropylmethylcellulose, pectins, inulin and its derivatives, starches and hydrolysates of starches of equivalent low dextrose, possibly hydrogenated, or even minerals.
  • the Applicant has evaluated its flowability using the device sold by the company HOSOKAWA.
  • This device makes it possible to measure, under standardized and reproducible conditions, the flowability of a powder and to calculate a flow rate also called Carr index.
  • the mannitol according to the invention usually has an excellent flow rate, between 70 and 90. This value is preferably between 75 and 90 and more preferably between 80 and 90. This value is very close to those of mannitol powders of the prior art obtained by wet granulation or by extrusion of crystals obtained by crystallization in water. This is all the more remarkable since, compared with these prior products, the pulverulent mannitol according to the invention has a much finer particle size.
  • the product's flowability subject of the invention is usually significantly higher than those of mannitol powders obtained by simple crystallization in water or simple atomization.
  • the excellent flowability of the mannitol of the invention is explained by the combination of several of its physicochemical characteristics, in particular its centered particle size, l absence of significant electrostatic charges on the surface of the particles constituting it, its richness in mannitol, its low hygroscopicity and finally the characteristic shape of the particles constituting it.
  • the pulverulent mannitol according to the invention comprises particles, of variable shape, always devoid of sharp edges and composed of a multitude of microparticles agglomerated together.
  • a mannitol crystallized in water consisting of particles, in the form of strata, of substantially constant thickness but of variable length and width. It is also different from a mannitol obtained by simple atomization composed of essentially spherical particles or else from an extruded product comprising angular particles in the form of fairly regular blocks.
  • a second essential functional property of the pulverulent mannitol in accordance with the invention is that of dissolving very quickly in water.
  • a test II which consists in introducing into 150 grams of demineralized and degassed water, maintained at 20 ° C. and subjected to stirring at 200 rpm in a beaker of 250 ml of form. low, exactly 5 grams of a particle size section of 100 to 200 microns of the product to be tested.
  • the dissolution time corresponds to the time required after introduction of the cut particle size to obtain perfect visual clarity of the suspension thus prepared.
  • the pulverulent mannitol according to the invention generally has a dissolution rate of less than 30 seconds.
  • the preferred product dissolves in less than 25 seconds while the ideal product requires a time of less than 20 seconds. These times are generally lower than those obtained with all the mannitol powders currently marketed.
  • the pulverulent mannitol according to the invention has a dispersibility generally between 10 and 30 and preferably between 10 and 25, which indicates a very low tendency to generate dust. It can be seen that the product of the invention has in this respect as good characteristics as the granulated or extruded powders of mannitol previously crystallized in water and of coarse particle size. On the other hand, its tendency to produce dust is much less than that of the powders obtained by simple crystallization in water or by simple atomization like that described in patent JP 61.85330.
  • the pulverulent mannitol according to the invention is capable of being obtained by carrying out a step of atomizing a relatively pure solution or suspension of mannitol respectively to the amount of sugars or of polyols present in the solution or the suspension, then to a wet granulation step of the mannitol resulting from said atomization step.
  • the product in accordance with the invention cannot be prepared by simple atomization as has already been done, or even by the granulation of mannitol crystals obtained by crystallization in water or another solvent such as alcohol.
  • the Applicant has found that the combination of atomization and granulation makes it possible, unlike the use of techniques known and applicable to mannitol, to adjust the friability so that it is high but not excessive, to adjust the density but also to prepare with high yield a product according to the invention in terms of its particle size.
  • syrup intended to be atomized may also include substances other than sugars or polyols, in particular when the latter are not subject to thermal degradation.
  • This suspension can without problem be micronized and / or heated to 140 ° C., taking into account the very high chemical stability of mannitol so as to adjust the size and the proportion of mannitol particles at the inlet of the atomizer.
  • the atomized powder is then granulated using either water or steam, or a mannitol syrup, or even, although this is not preferred, a syrup comprising a binder such as a polyvinylpyrolidone, gum arabic, a hydroxypropylmethylcellulose, a maltodextrin, a pregelified starch, a gelatin or any other binder known by a person skilled in the art to possess the required properties.
  • a binder such as a polyvinylpyrolidone, gum arabic, a hydroxypropylmethylcellulose, a maltodextrin, a pregelified starch, a gelatin or any other binder known by a person skilled in the art to possess the required properties.
  • the adequate water content is generally of the order of 10 to 20%, but may vary with the particle size of the atomized powder.
  • a syrup comprising a binder
  • the latter represents from 0.1 to 15%, preferably from 0.5 to 4%, of the dry matter of the pulverulent mannitol according to the invention.
  • a binder is preferably chosen which is not capable of altering the particularly advantageous property of mannitol of not being cariogenic.
  • the simplest and preferred way to do this is to use the same syrup as a binder as that intended for atomization, as certain industrial devices allow, successively atomizing and then granulating.
  • the mannitol according to the invention can be used as a basic product for the preparation of chemicals such as, for example, flame retardants, polyurethane foams, antifreezes, surfactants, plasticizer or filler, such as in plastics, paints , resins, rubbers or papers, or a product intended to support or shape, for example veterinary or phytosanitary principles, industrial enzymes, fertilizers, trace elements, pesticides, active agents allowing destruction rodents or harmful mammals.
  • chemicals such as, for example, flame retardants, polyurethane foams, antifreezes, surfactants, plasticizer or filler, such as in plastics, paints , resins, rubbers or papers, or a product intended to support or shape, for example veterinary or phytosanitary principles, industrial enzymes, fertilizers, trace elements, pesticides, active agents allowing destruction rodents or harmful mammals.
  • chemicals such as, for example, flame retardants, polyurethane foams, antifreezes, surfactants, plasticizer or filler, such as in
  • aqueous solution of mannitol containing 40% of matter is prepared by dissolving mannitol crystals obtained by crystallization from water at 75 ° C.
  • the pulverulent mannitol according to the invention has the properties of a good excipient, namely has moderate and not excessive friability, good flowability, very high solubilization speed.
  • This excipient has the advantage of being neither cariogenic nor hygroscopic.
  • pulverulent products in accordance with the invention are prepared by applying the process described in example 1 but by modifying slightly the temperatures, the dry solids of entry, and the atomization flows but also the granulation conditions so as to obtain a range of samples.
  • the products obtained have the characteristics set out in the table below.
  • the products according to the invention all have, unlike the products of the prior art, excellent functional properties, thus making them suitable for use without disadvantage as excipients and carriers of non-cariogenic and non-hygroscopic additives, in particular in food and pharmaceutical industry.
  • the product according to the invention advantageously makes it possible to obtain harder tablets than with the various compressible products based on lactose or sucrose commonly used in this application.
  • the pulverulent mannitol according to the invention constitutes an excellent directly compressible product unlike mannitol crystallized in water, and an excellent excipient for the most diverse active principles and in particular those sensitive to humidity such as for example certain enzymes or vitamins.

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  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Organic Chemistry (AREA)
  • Public Health (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Epidemiology (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Molecular Biology (AREA)
  • Veterinary Medicine (AREA)
  • Biophysics (AREA)
  • Medicinal Chemistry (AREA)
  • Nutrition Science (AREA)
  • Engineering & Computer Science (AREA)
  • Food Science & Technology (AREA)
  • Polymers & Plastics (AREA)
  • Medicinal Preparation (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Seasonings (AREA)
  • Peptides Or Proteins (AREA)
  • General Preparation And Processing Of Foods (AREA)
EP94402134A 1993-09-28 1994-09-26 Mannitol pulvérulent de friabilité modérée et son procédé de préparation Expired - Lifetime EP0645096B1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
FR9311513 1993-09-28
FR9311513A FR2710637B1 (fr) 1993-09-28 1993-09-28 Mannitol pulvérulent de friabilité modérée et son procédé de préparation.

Publications (2)

Publication Number Publication Date
EP0645096A1 EP0645096A1 (fr) 1995-03-29
EP0645096B1 true EP0645096B1 (fr) 1997-12-03

Family

ID=9451298

Family Applications (1)

Application Number Title Priority Date Filing Date
EP94402134A Expired - Lifetime EP0645096B1 (fr) 1993-09-28 1994-09-26 Mannitol pulvérulent de friabilité modérée et son procédé de préparation

Country Status (16)

Country Link
US (1) US5573777A (ja)
EP (1) EP0645096B1 (ja)
JP (1) JP3492428B2 (ja)
KR (1) KR100353433B1 (ja)
CN (1) CN1046622C (ja)
AT (1) ATE160676T1 (ja)
AU (1) AU675732B2 (ja)
CA (1) CA2133012C (ja)
DE (1) DE69407123T2 (ja)
DK (1) DK0645096T3 (ja)
ES (1) ES2109635T3 (ja)
FI (1) FI112356B (ja)
FR (1) FR2710637B1 (ja)
GR (1) GR3025720T3 (ja)
HU (1) HU217453B (ja)
NO (1) NO302356B1 (ja)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2011027061A1 (fr) 2009-09-01 2011-03-10 Roquette Freres Procede de remplacement total ou partiel du talc dans les chewing-gums
EP1138661B2 (fr) † 2000-03-29 2013-11-20 Roquette Frères Mannitol pulvérulent et son procédé de préparation

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US6235947B1 (en) * 1997-04-14 2001-05-22 Takeda Chemical Industries, Ltd. D-mannitol and its preparation
HUP9902165A3 (en) 1996-04-16 2001-01-29 Bayer Ag D-mannit and with big specific surface area process for preparing it and solid pharmaceuticals containing it
DE19615418A1 (de) * 1996-04-22 1997-10-23 Merck Patent Gmbh Polyol-Zusammensetzung
DE19617487A1 (de) † 1996-05-02 1997-11-06 Merck Patent Gmbh Geschmacksverbesserung von Arzneimittelwirkstoffen
US6024981A (en) * 1997-04-16 2000-02-15 Cima Labs Inc. Rapidly dissolving robust dosage form
GB9716432D0 (en) * 1997-08-05 1997-10-08 Cerestar Holding Bv Tableting of erythritol
DE19819012A1 (de) * 1998-04-29 1999-11-25 Dynamit Nobel Ag Feuersichere, nicht explosionsfähige, Nitroglycerin und wasserfreie Lactose enthaltende Feststoffmischungen
US6296868B1 (en) * 1998-11-19 2001-10-02 Advanced Technology Pharmaceuticals Corporation Chewable tablets containing mannitol and aspartame
FR2787110B1 (fr) † 1998-12-11 2001-02-16 Roquette Freres Sorbitol pulverulent et son procede de preparation
US20020071864A1 (en) * 1999-03-25 2002-06-13 Yuhan Corporation Rapidly disintegrable tablet for oral administration
CA2342121C (fr) * 2000-03-29 2010-05-25 Roquette Freres Mannitol pulverulent et son procede de preparation
DE60139339D1 (de) * 2000-11-07 2009-09-03 Novartis Vaccines & Diagnostic Stabilisierte interferonzusammensetzungen
CN1239151C (zh) * 2001-03-06 2006-02-01 协和发酵工业株式会社 口腔内快速崩解片剂
DE10161402A1 (de) * 2001-12-13 2003-06-18 Merck Patent Gmbh Verfahren zur Herstellung von direkt tablettierbarem beta-Mannit
US7118765B2 (en) 2001-12-17 2006-10-10 Spi Pharma, Inc. Co-processed carbohydrate system as a quick-dissolve matrix for solid dosage forms
JP4808960B2 (ja) 2002-05-14 2011-11-02 エフ エム シー コーポレーション 微結晶質セルロース組成物
ES2199061B1 (es) * 2002-06-10 2005-02-16 Laboratorios Vita, S.A. Comprimidos bucodispersables y procedimiento para su obtencion.
US20040109889A1 (en) * 2002-12-04 2004-06-10 Bunick Frank J. Surface treatment composition for soft substrates
US7282217B1 (en) * 2003-08-29 2007-10-16 Kv Pharmaceutical Company Rapidly disintegrable tablets
WO2007034287A2 (en) * 2005-09-19 2007-03-29 University Of The Witwatersrand, Johannesburg Oramucosal pharmaceutical dosage form
US7879382B2 (en) * 2005-09-30 2011-02-01 Fmc Corporation Stabilizers and compositions and products comprising same
US20100221333A1 (en) * 2005-12-21 2010-09-02 Burkard Schlutermann Pellets Comprising a Core With a Water-Soluble Carrier
EP2076249A2 (en) * 2006-10-27 2009-07-08 FMC Corporation Dry granulation binders, products, and use thereof
GB2450498A (en) 2007-06-26 2008-12-31 Schlumberger Holdings Battery powered rotary steerable drilling system
JP5650532B2 (ja) 2008-08-18 2015-01-07 三菱商事フードテック株式会社 新規マンニトール打錠用賦形剤
EP2385769A4 (en) * 2008-12-15 2014-08-20 Valeant Pharmaceuticals Luxembourg S R L QUICKLY SOLUBLE VITAMIN FORMULATION AND METHOD FOR THEIR USE
FR2949462B1 (fr) * 2009-09-01 2011-12-16 Roquette Freres Poudre de cristaux de mannitol define, son procede de fabrication
WO2012049156A1 (en) 2010-10-12 2012-04-19 Bayer Animal Health Gmbh Non-starch based soft chewables
CN103842425B (zh) 2011-10-05 2017-05-24 Fmc有限公司 微晶纤维素和羧甲基纤维素的稳定剂组合物、制备方法和应用
ES2657648T3 (es) 2011-10-05 2018-03-06 Fmc Corporation Composición estabilizadora de celulosa microcristalina y carboximetilcelulosa co-reducida, método para elaborarla y usos
WO2013085810A2 (en) 2011-12-09 2013-06-13 Fmc Corporation Co-attrited stabilizer composition
BE1021954B1 (nl) 2014-06-05 2016-01-28 Syral Belgium Nv Samenstelling van sorbitol met lage friabiliteit
DK3263110T3 (da) * 2015-02-26 2023-07-31 Takeda Pharmaceuticals Co Tablet, som omfatter et methoxyurinstofderivat og mannitolpartikler
FR3038836B1 (fr) * 2015-07-17 2017-07-14 Roquette Freres Granules de mannitol pour compression directe

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FR2571045B1 (fr) * 1984-10-03 1987-12-11 Roquette Freres Mannitol granulaire directement compressible et son procede de fabrication
FR2571046B1 (fr) * 1984-10-03 1987-10-16 Roquette Freres Procede de preparation de mannitol granulaire directement compressible
JPS6185330A (ja) * 1984-10-04 1986-04-30 Fuji Kagaku Kogyo Kk 直打用賦形薬の製造法
JPS6185331A (ja) * 1984-10-04 1986-04-30 Fuji Kagaku Kogyo Kk 直打用賦形薬の製造法
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Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1138661B2 (fr) † 2000-03-29 2013-11-20 Roquette Frères Mannitol pulvérulent et son procédé de préparation
WO2011027061A1 (fr) 2009-09-01 2011-03-10 Roquette Freres Procede de remplacement total ou partiel du talc dans les chewing-gums

Also Published As

Publication number Publication date
JP3492428B2 (ja) 2004-02-03
AU7423994A (en) 1995-04-13
FI944464A0 (fi) 1994-09-27
FR2710637B1 (fr) 1995-12-08
CA2133012C (en) 2006-01-31
DK0645096T3 (da) 1998-05-04
CN1046622C (zh) 1999-11-24
KR100353433B1 (ko) 2002-12-11
DE69407123T2 (de) 1998-04-23
ES2109635T3 (es) 1998-01-16
ATE160676T1 (de) 1997-12-15
GR3025720T3 (en) 1998-03-31
JPH07184590A (ja) 1995-07-25
HU217453B (hu) 2000-01-28
CN1107516A (zh) 1995-08-30
NO943586L (no) 1995-03-29
EP0645096A1 (fr) 1995-03-29
NO302356B1 (no) 1998-02-23
HU9402773D0 (en) 1994-12-28
DE69407123D1 (de) 1998-01-15
US5573777A (en) 1996-11-12
KR950008457A (ko) 1995-04-17
HUT70804A (en) 1995-11-28
CA2133012A1 (en) 1995-03-29
FI944464A (fi) 1995-03-29
FR2710637A1 (fr) 1995-04-07
FI112356B (fi) 2003-11-28
AU675732B2 (en) 1997-02-13
NO943586D0 (no) 1994-09-27

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